Details Top

Internal ID UUID643fe59a3ef87765148482
Scientific name Origanum syriacum
Authority L.
First published in Sp. Pl. : 590 (1753)

Ethnobotanical Use Top

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Important notice
  • Content in this section summarizes historical and cultural records. It is not medical advice.
  • Do not use plants for self-treatment. Safety, efficacy, and appropriate use are not established here.
  • Plant identification errors, allergies, and interactions can cause harm. Consult qualified professionals for health questions.
  • Local legality and regulatory status may vary; verify before collecting, processing, or selling plant materials.

Origanum syriacum L. (Syrian oregano) is widely gathered and cultivated in the Levant for both culinary and medicinal purposes. In Palestine and Israel, the herb—locally called za’atar—is dried and the leaves are steeped in hot water to make a tea used for coughs, colds, and general digestive complaints, with preparations documented by Ethnomedicine Field Research and by Neilson’s 2012 report from the SRTES “Syrian Oregano” project. Among Syrian, Lebanese, and Jordanian communities, dried leaf infusions are similarly employed for respiratory and digestive relief, including a rosewater-scented “za’atar tea” with lemon noted by Taqi (2014) in Jordanian ethnobotany. In Cyprus, where the species occurs as a wild subspecies, folk use includes leaf infusions for colds and indigestion, as recorded by Arnold-Apostolides (1991). Decoctions of leaves and tops are less common, but local reports from Palestinian hamlets describe short decoctions for coughs and sore throats (Batanouny, 1999).

A practical leaf tea can be made as follows: steep 1 to 2 teaspoons (about 1–2 g) of dried crushed leaves in 200 ml of near-boiling water for 5 to 7 minutes, then strain and drink while warm up to 2 cups daily. Reports from Jordan and Palestine note occasional additions of honey or lemon to soothe sore throats (Taqi, 2014; SRTES, 2012). Do not exceed moderate daily doses; because this species shares high phenolic content and strong essential oils with other Origanum species, people taking anticoagulants or with bleeding disorders should use caution, and pregnant or nursing individuals should limit intake or avoid medicinal doses without professional guidance.

Phytochemistry consistent with this use profile includes carvacrol and thymol as major constituents in the essential oil (Baser, 2008), together with flavonoids (e.g., luteolin and apigenin derivatives) and rosmarinic acid—antioxidant and phenolic compounds documented for Origanum syriacum and implicated in the plant’s well-established antimicrobial and spasmolytic activity.

Ongoing research supports modest antioxidant and antimicrobial effects (Baser, 2008; Hadjikakou et al., 2017), and dried za’atar, whole-leaf teas, and leaf-infused olive oil remain commercially and culturally available across the Levant and diaspora communities (SRTES, 2012; Taqi, 2014).

General Uses Top

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Common products:
• Dried leaves used as a culinary spice/herb in Middle Eastern cuisine.
• Leaves and stems sold as “Syrian oregano,” “za’atar oregano,” and “bible hyssop.”
• Essential oil (carvacrol-rich) used as a flavoring agent in foods and a fragrance in cosmetics and soaps.

Industrial and craft applications:
• No wood or fiber uses. The aerial parts may be used as dried potpourri or in sachets for fragrance.

Food and beverages (non-medicinal):
• Leaves harvested before flowering, dried, and mechanically cleaned; used as a seasoning in spice blends and as a single-herb product.
• Fresh or dried leaves incorporated as a culinary herb.
• Essential oil used at very low levels as a natural flavoring in foods; concentration determined by flavor objectives and flavoring law.

Colorants and tanning:
• No documented dyes or tannins from this species.

Wood and fiber:
• No wood, timber, or fiber products. Plant is herbaceous.

Fragrance and cosmetics:
• Essential oil used as a fragrance in soaps and toiletries; dose limited by safety and IFRA/ISO guidance for essential oils.

Properties relevant to use:
• Leaves yield an essential oil typically rich in carvacrol, with thymol and p-cymene as common minor constituents.
• The aromatic profile is characterized by a strong, warm, thyme-like note derived from carvacrol.
• Flavorants and fragrances must comply with identity and purity requirements for natural essential oils.

Standards and regulation:
• Dried spice: marketed under international spice nomenclature and quality standards for dried herbs.
• Essential oil: governed by IFRA Standards and ISO 3216 for essential oils; in cosmetics, formulations must meet safety requirements under EU Cosmetics Regulation or comparable national frameworks.
• Food flavorings are controlled by specific flavoring regulations and maximum use levels.

Sustainability and sourcing:
• The species is predominantly wild-harvested, raising concerns about habitat pressure in parts of its range; cultivated supply and sustainable wild-collection initiatives can mitigate impacts.

Synonyms Top

Scientific name Authority First published in
Majorana syriaca (L.) Raf. Autik. Bot. : 119 (1840)
Schizocalyx syriacus (L.) Scheele Flora 26: 575. 1843

Common names Top

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Language Common/alternative name
English biblical-hyssop
English majorana syriaca
English biblical hyssop
English bible hyssop
English lebanese oregano
English syrian oregano
Arabic زعتر
Arabic مردقوش سوري
Bulgarian сирийски риган
Persian اوریگانوم سیراکام
Hebrew אזוב מצוי
Hebrew צעתר
Japanese シリアンオレガノ
Korean 시리아오레가노
Polish lebiodka syryjska
Russian душица сирийская
Russian majorana syriaca
Swedish syrisk oregano
Ukrainian Затар
Ukrainian Материнка сирійська

Subspecies (abbr. subsp./ssp.) Top

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Name Authority First published in
Origanum syriacum subsp. bevanii (Holmes) Greuter & Burdet Willdenowia 14: 301 (1984 publ. 1985)
Origanum syriacum subsp. sinaicum (Boiss.) Greuter & Burdet Willdenowia 14: 301 (1984 publ. 1985)
Origanum syriacum subsp. syriacum Unknown

Varieties (abbr. var.) Top

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No variety added yet.

Subvarieties (abbr. subvar.) Top

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Forms (abbr. f.) Top

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Germination/Propagation Top

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No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Asia-temperate
    • Arabian Peninsula
      • Saudi Arabia
    • Western Asia
      • Cyprus
      • Lebanon-Syria
      • Palestine
      • Sinai
      • Turkey

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000260740
Tropicos 100234908
KEW urn:lsid:ipni.org:names:453375-1
The Plant List kew-143930
Missouri Botanical Garden 257125
Open Tree Of Life 731839
NCBI Taxonomy 1082757
IPNI 453375-1
iNaturalist 340456
GBIF 6411178
Freebase /m/0t52kt4
EPPO ORISY
EOL 483861
USDA GRIN 448310
Wikipedia Origanum_syriacum

Genomes (via NCBI) Top

No reference genome is available on NCBI yet. We are constantly monitoring for new data.

Scientific Literature Top

Below are displayed the latest 15 articles published in PMC (PubMed Central®) and other sources (DOI number only)!
If you wish to see all the related articles click here.
Title Authors Publication Released IDs
Re‐evaluation of certain aspects of the EFSA Scientific Opinion of April 2010 on risk assessment of parasites in fishery products, based on new scientific data. Part 1: ToRs1–3 Koutsoumanis K, Allende A, Alvarez‐Ordóñez A, Bover‐Cid S, Chemaly M, De Cesare A, Herman L, Hilbert F, Lindqvist R, Nauta M, Nonno R, Peixe L, Ru G, Simmons M, Skandamis P, Suffredini E, Buchmann K, Careche M, Levsen A, Mattiucci S, Mladineo I, Santos MJ, Barcia‐Cruz R, Broglia A, Chuzhakina K, Goudjihounde SM, Guerra B, Messens W, Guajardo IM, Bolton D EFSA J 22-Apr-2024
PMCID:PMC11033839
doi:10.2903/j.efsa.2024.8719
PMID:38650612
Potential therapeutic targets of the JAK2/STAT3 signaling pathway in triple-negative breast cancer Long L, Fei X, Chen L, Yao L, Lei X Front Oncol 18-Apr-2024
PMCID:PMC11063389
doi:10.3389/fonc.2024.1381251
PMID:38699644
Nutritional and Physiological Properties of Thymbra spicata: In Vitro Study Using Fecal Fermentation and Intestinal Integrity Models Khalil M, Piccapane F, Vacca M, Celano G, Mahdi L, Perniola V, Apa CA, Annunziato A, Iacobellis I, Procino G, Calasso M, De Angelis M, Caroppo R, Portincasa P Nutrients 21-Feb-2024
PMCID:PMC10934825
doi:10.3390/nu16050588
PMID:38474717
Use of Essential Oils to Counteract the Phenomena of Antimicrobial Resistance in Livestock Species Lupia C, Castagna F, Bava R, Naturale MD, Zicarelli L, Marrelli M, Statti G, Tilocca B, Roncada P, Britti D, Palma E Antibiotics (Basel) 07-Feb-2024
PMCID:PMC10885947
doi:10.3390/antibiotics13020163
PMID:38391549
Effects of essential oils on egg production and feed efficiency as influenced by laying hen breed: A meta-analysis Darmawan A, Öztürk E, Güngör E, Özlü Ş, Jayanegara A Vet World 23-Jan-2024
PMCID:PMC10884582
doi:10.14202/vetworld.2024.197-206
PMID:38406358
Phytochemical Profile, GC-MS Profiling and In Vitro Evaluation of Some Biological Applications of the Extracts of Origanum syriacum L. and Cousinia libanotica D.C. Dawra M, Bouajila J, El Beyrouthy M, Taillandier P, Nehme N, El Rayess Y Plants (Basel) 03-Jan-2024
PMCID:PMC10780604
doi:10.3390/plants13010137
PMID:38202445
Ethnomedicinal evaluation of medicinal plants used for therapies by men and women in rural and urban communities in Makkah district Qari SH, Alqethami A, Qumsani AT Saudi Pharm J 02-Dec-2023
PMCID:PMC10733703
doi:10.1016/j.jsps.2023.101881
PMID:38130903
Antimicrobial Potential of Different Isolates of Chaetomium globosum Combined with Liquid Chromatography Tandem Mass Spectrometry Chemical Profiling Goda MS, El-Kattan N, Abdel-Azeem MA, Allam KA, Badr JM, Nassar NA, Almalki AJ, Alharbi M, Elhady SS, Eltamany EE Biomolecules 21-Nov-2023
PMCID:PMC10742071
doi:10.3390/biom13121683
PMID:38136556
The significance of essential oils and their antifungal properties in the food industry: A systematic review Abdi-Moghadam Z, Mazaheri Y, Rezagholizade-shirvan A, Mahmoudzadeh M, Sarafraz M, Mohtashami M, Shokri S, Ghasemi A, Nickfar F, Darroudi M, Hossieni H, Hadian Z, Shamloo E, Rezaei Z Heliyon 29-Oct-2023
PMCID:PMC10637975
doi:10.1016/j.heliyon.2023.e21386
PMID:37954273
Proposed mechanisms of action of herbal drugs and their biologically active constituents in the treatment of coughs: an overview Pourova J, Dias P, Pour M, Bittner Fialová S, Czigle S, Nagy M, Tóth J, Balázs VL, Horváth A, Csikós E, Farkas Á, Horváth G, Mladěnka P PeerJ 24-Oct-2023
PMCID:PMC10607228
doi:10.7717/peerj.16096
PMID:37901462
Enhanced Natural Strength: Lamiaceae Essential Oils and Nanotechnology in In Vitro and In Vivo Medical Research Kowalczyk T, Merecz-Sadowska A, Ghorbanpour M, Szemraj J, Piekarski J, Bijak M, Śliwiński T, Zajdel R, Sitarek P Int J Mol Sci 17-Oct-2023
PMCID:PMC10607815
doi:10.3390/ijms242015279
PMID:37894959
Effects of Origanum majorana on Breast Cancer Cells: An Alternative to Chemotherapy? Sanders Z, Moffitt BA, Treaster M, Larkins A, Khulordava N, Benjock J, Spencer J, Henrie K, Wurst MJ, Broom A, Tamez N, DeRosa G, Campbell M, Keller E, Powell A, Weinbrenner D, Abenavoli L, Edenfield WJ, Chung K, Boccuto L, Ivankovic D Metabolites 16-Oct-2023
PMCID:PMC10608860
doi:10.3390/metabo13101083
PMID:37887408
Anti-oomycete activities from essential oils and their major compounds on Phytophthora infestans Deweer C, Sahmer K, Muchembled J Environ Sci Pollut Res Int 02-Oct-2023
PMCID:PMC10625517
doi:10.1007/s11356-023-29270-6
PMID:37779122
Antioxidant, Antiglaucoma, Anticholinergic, and Antidiabetic Effects of Kiwifruit (Actinidia deliciosa) Oil: Metabolite Profile Analysis Using LC-HR/MS, GC/MS and GC-FID Ozden EM, Bingol Z, Mutlu M, Karagecili H, Köksal E, Goren AC, Alwasel SH, Gulcin İ Life (Basel) 20-Sep-2023
PMCID:PMC10532620
doi:10.3390/life13091939
PMID:37763342
Mediterranean Plants as Potential Source of Biopesticides: An Overview of Current Research and Future Trends Fragkouli R, Antonopoulou M, Asimakis E, Spyrou A, Kosma C, Zotos A, Tsiamis G, Patakas A, Triantafyllidis V Metabolites 22-Aug-2023
PMCID:PMC10535963
doi:10.3390/metabo13090967
PMID:37755247

Phytochemical Profile Top

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Below are displayed the proven (via scientific papers) natural compounds!
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Name PubChem ID Canonical SMILES MW Found in Proof
> Hydrocarbons / Unsaturated hydrocarbons / Branched unsaturated hydrocarbons
Gamma-Terpinene 7461 Click to see 136.23 unknown https://doi.org/10.1034/J.1399-3054.1992.840320.X
https://doi.org/10.3109/13880209109082875
https://doi.org/10.1080/10412905.1991.9697923
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acid esters
Methyl 2-methylbutyrate 13357 Click to see CCC(C)C(=O)OC 116.16 unknown https://doi.org/10.1080/10412905.1991.9697923
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohol esters
Citronellyl butyrate 8835 Click to see CCCC(=O)OCCC(C)CCC=C(C)C 226.35 unknown https://doi.org/10.1080/10412905.1991.9697923
Geranyl butyrate 5355856 Click to see CCCC(=O)OCC=C(C)CCC=C(C)C 224.34 unknown https://doi.org/10.1080/10412905.1991.9697923
Geranyl hexanoate 5365992 Click to see 252.39 unknown https://doi.org/10.1080/10412905.1991.9697923
Geranyl propionate 5355853 Click to see 210.31 unknown https://doi.org/10.1080/10412905.1991.9697923
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols
1-Octen-3-Ol 18827 Click to see 128.21 unknown https://doi.org/10.3109/13880209109082875
https://doi.org/10.1080/10412905.1991.9697923
3-Octanol 11527 Click to see 130.23 unknown https://doi.org/10.1080/10412905.1991.9697923
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
5,9-Dimethyl-4,8-decadienoic acid 6365434 Click to see CC(=CCCC(=CCCC(=O)O)C)C 196.29 unknown https://doi.org/10.1080/10412905.1991.9697923
beta-Ocimene, (3Z)- 5320250 Click to see 136.23 unknown https://doi.org/10.3109/13880209109082875
Citronellol 8842 Click to see 156.26 unknown https://doi.org/10.1080/10412905.1991.9697923
Geraniol 637566 Click to see CC(=CCCC(=CCO)C)C 154.25 unknown https://doi.org/10.1080/10412905.1991.9697923
Linalool 6549 Click to see 154.25 unknown https://doi.org/10.1080/10412905.1991.9697923
https://doi.org/10.1055/S-2007-969862
Linalyl Acetate 8294 Click to see 196.29 unknown https://doi.org/10.3109/13880209109082875
Myrcene 31253 Click to see 136.23 unknown https://doi.org/10.1080/10412905.1991.9697923
https://doi.org/10.1055/S-2007-969862
https://doi.org/10.3109/13880209109082875
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Aromatic monoterpenoids
Carvacrol 10364 Click to see CC1=C(C=C(C=C1)C(C)C)O 150.22 unknown https://doi.org/10.1055/S-2007-969862
https://doi.org/10.3109/13880209109082875
https://doi.org/10.1080/10412905.1991.9697923
Carvacryl acetate 80792 Click to see 192.25 unknown https://doi.org/10.3109/13880209109082875
Carvacryl methyl ether 80790 Click to see 164.24 unknown https://doi.org/10.3109/13880209109082875
P-Cymene 7463 Click to see 134.22 unknown https://doi.org/10.1034/J.1399-3054.1992.840320.X
https://doi.org/10.1080/10412905.1991.9697923
Thymol 6989 Click to see 150.22 unknown https://doi.org/10.1080/10412905.1991.9697923
https://doi.org/10.3109/13880209109082875
https://doi.org/10.1055/S-2007-969862
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
(+-)-alpha-Pinene 6654 Click to see 136.23 unknown https://doi.org/10.3109/13880209109082875
https://doi.org/10.1080/10412905.1991.9697923
(5S)-4-methylidene-1-propan-2-ylbicyclo[3.1.0]hexane 6429260 Click to see 136.23 unknown https://doi.org/10.3109/13880209109082875
3-Carene 26049 Click to see CC1=CCC2C(C1)C2(C)C 136.23 unknown https://doi.org/10.1055/S-2007-969862
https://doi.org/10.3109/13880209109082875
alpha-Thujene 17868 Click to see 136.23 unknown https://doi.org/10.1080/10412905.1991.9697923
Beta-Pinene 14896 Click to see 136.23 unknown https://doi.org/10.1080/10412905.1991.9697923
https://doi.org/10.3109/13880209109082875
Borneol 64685 Click to see 154.25 unknown https://doi.org/10.1080/10412905.1991.9697923
Camphene 6616 Click to see 136.23 unknown https://doi.org/10.1080/10412905.1991.9697923
https://doi.org/10.1055/S-2007-969862
https://doi.org/10.3109/13880209109082875
Camphor 2537 Click to see 152.23 unknown https://doi.org/10.1080/10412905.1991.9697923
https://doi.org/10.1055/S-2007-969862
Sabinene 18818 Click to see 136.23 unknown https://doi.org/10.3109/13880209109082875
Tricyclene 79035 Click to see 136.23 unknown https://doi.org/10.1080/10412905.1991.9697923
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
(-)-cis-Carveol 330573 Click to see CC1=CCC(CC1O)C(=C)C 152.23 unknown https://doi.org/10.1080/10412905.1991.9697923
1,6-Dihydrocarvone 24473 Click to see 152.23 unknown https://doi.org/10.1080/10412905.1991.9697923
4-Terpineol, (+/-)- 11230 Click to see CC1=CCC(CC1)(C(C)C)O 154.25 unknown https://doi.org/10.1080/10412905.1991.9697923
alpha-PHELLANDRENE 7460 Click to see 136.23 unknown https://doi.org/10.1080/10412905.1991.9697923
Alpha-Terpinene 7462 Click to see 136.23 unknown https://doi.org/10.1080/10412905.1991.9697923
Alpha-Terpineol 17100 Click to see 154.25 unknown https://doi.org/10.1080/10412905.1991.9697923
Beta-Phellandrene 11142 Click to see CC(C)C1CCC(=C)C=C1 136.23 unknown https://doi.org/10.3109/13880209109082875
https://doi.org/10.1080/10412905.1991.9697923
Carvone, (+)- 16724 Click to see CC1=CCC(CC1=O)C(=C)C 150.22 unknown https://doi.org/10.1080/10412905.1991.9697923
Limonene, (+/-)- 22311 Click to see CC1=CCC(CC1)C(=C)C 136.23 unknown https://doi.org/10.1055/S-2007-969862
https://doi.org/10.1080/10412905.1991.9697923
https://doi.org/10.3109/13880209109082875
Terpinolene 11463 Click to see 136.23 unknown https://doi.org/10.3109/13880209109082875
https://doi.org/10.1080/10412905.1991.9697923
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
alpha-Guaiene 5317844 Click to see 204.35 unknown https://doi.org/10.1080/10412905.1991.9697923
Caryophyllene 5281515 Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C 204.35 unknown https://doi.org/10.1080/10412905.1991.9697923
https://doi.org/10.1055/S-2007-969862
Humulene 5281520 Click to see 204.35 unknown https://doi.org/10.1080/10412905.1991.9697923
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides
(2R,3S,4S,5R,6S)-2-(hydroxymethyl)-6-(2-hydroxy-4-methyl-1-propan-2-ylcyclohex-3-en-1-yl)oxyoxane-3,4,5-triol 129716291 Click to see 332.39 unknown https://doi.org/10.1016/S0031-9422(01)00386-7
(2R,3S,4S,5R,6S)-2-(hydroxymethyl)-6-[2-methyl-5-propan-2-yl-4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenoxy]oxane-3,4,5-triol 11092169 Click to see 490.50 unknown https://doi.org/10.1016/S0031-9422(01)00386-7
(2R,3S,4S,5S,6S)-2-(hydroxymethyl)-6-[(1R,2S)-2-hydroxy-4-methyl-1-propan-2-ylcyclohex-3-en-1-yl]oxyoxane-3,4,5-triol 163043443 Click to see 332.39 unknown https://doi.org/10.1016/S0031-9422(01)00386-7
Zataroside A 25102046 Click to see 328.36 unknown https://doi.org/10.1016/S0031-9422(01)00386-7
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Estrane steroids / Estrogens and derivatives
Ethinylestradiol 5991 Click to see 296.40 unknown https://doi.org/10.1080/10412905.1991.9697923
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
(2R,3S,4S,5R,6S)-2-(hydroxymethyl)-6-(4-hydroxy-2-methyl-3-propan-2-ylphenoxy)oxane-3,4,5-triol 101203410 Click to see CC1=C(C=CC(=C1C(C)C)O)OC2C(C(C(C(O2)CO)O)O)O 328.36 unknown https://doi.org/10.1016/S0031-9422(01)00386-7
(2R,3S,4S,5R,6S)-2-(hydroxymethyl)-6-(4-hydroxy-3-methyl-2-propan-2-ylphenoxy)oxane-3,4,5-triol 101203411 Click to see 328.36 unknown https://doi.org/10.1016/S0031-9422(01)00386-7
(2S,3R,4S,5R)-2-[(2R,3S,4R,5R,6S)-4,5-dihydroxy-6-(hydroxymethyl)-2-(2-methyl-5-propan-2-ylphenoxy)oxan-3-yl]oxyoxane-3,4,5-triol 163195302 Click to see CC1=C(C=C(C=C1)C(C)C)OC2C(C(C(C(O2)CO)O)O)OC3C(C(C(CO3)O)O)O 444.50 unknown https://doi.org/10.1016/S0031-9422(01)00386-7
(2S,3R,4S,5S,6R)-2-[(2S,3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-2-(2-methyl-5-propan-2-ylphenoxy)oxan-3-yl]oxy-6-(hydroxymethyl)oxane-3,4,5-triol 101203408 Click to see 474.50 unknown https://doi.org/10.1016/S0031-9422(01)00386-7
Zataroside B 14589106 Click to see 328.36 unknown https://doi.org/10.1016/S0031-9422(01)00386-7
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Cinnamic acid esters
Ethyl 3-phenylprop-2-enoate 7649 Click to see 176.21 unknown https://doi.org/10.1080/10412905.1991.9697923

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